DE2340741A1 - Fungizid - Google Patents
FungizidInfo
- Publication number
- DE2340741A1 DE2340741A1 DE19732340741 DE2340741A DE2340741A1 DE 2340741 A1 DE2340741 A1 DE 2340741A1 DE 19732340741 DE19732340741 DE 19732340741 DE 2340741 A DE2340741 A DE 2340741A DE 2340741 A1 DE2340741 A1 DE 2340741A1
- Authority
- DE
- Germany
- Prior art keywords
- fungicide
- benzene
- leaves
- thiophanate
- diisopropyl ester
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000417 fungicide Substances 0.000 title claims description 11
- 230000000855 fungicidal effect Effects 0.000 title claims description 9
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims description 16
- -1 Butylcarbamoyl Chemical group 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- ZDQWESQEGGJUCH-UHFFFAOYSA-N Diisopropyl adipate Chemical compound CC(C)OC(=O)CCCCC(=O)OC(C)C ZDQWESQEGGJUCH-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- AJDLNNYMWNWZOE-UHFFFAOYSA-N benzene methyl N-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate Chemical compound c1ccccc1.COC(=O)NC(=S)Nc1ccccc1NC(=S)NC(=O)OC AJDLNNYMWNWZOE-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 13
- 239000003921 oil Substances 0.000 description 9
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 8
- 241000221785 Erysiphales Species 0.000 description 7
- 239000006013 carbendazim Substances 0.000 description 7
- AGSGXQFKXGFITI-UHFFFAOYSA-N dipropan-2-yl 1-nitrocyclohexa-3,5-diene-1,3-dicarboxylate Chemical compound CC(C)OC(=O)C1=CC=CC([N+]([O-])=O)(C(=O)OC(C)C)C1 AGSGXQFKXGFITI-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 230000002538 fungal effect Effects 0.000 description 3
- 238000011534 incubation Methods 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- 150000002790 naphthalenes Chemical class 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 241000221787 Erysiphe Species 0.000 description 2
- 241000510928 Erysiphe necator Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 244000141359 Malus pumila Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000009109 curative therapy Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical class CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000896242 Podosphaera Species 0.000 description 1
- 241001337928 Podosphaera leucotricha Species 0.000 description 1
- 241000896203 Podosphaera pannosa Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 241000109329 Rosa xanthina Species 0.000 description 1
- 235000004789 Rosa xanthina Nutrition 0.000 description 1
- 241000270295 Serpentes Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 235000021016 apples Nutrition 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- WVUDKDYNUGSTSE-UHFFFAOYSA-N dipropan-2-yl 2-nitrobenzene-1,3-dicarboxylate Chemical compound [N+](=O)([O-])C1=C(C(=O)OC(C)C)C=CC=C1C(=O)OC(C)C WVUDKDYNUGSTSE-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 210000002741 palatine tonsil Anatomy 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/48—Nitro-carboxylic acids; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (19)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732340741 DE2340741A1 (de) | 1973-08-11 | 1973-08-11 | Fungizid |
| JP49082321A JPS5088228A (enrdf_load_stackoverflow) | 1973-08-11 | 1974-07-19 | |
| US05/493,099 US3954993A (en) | 1973-08-11 | 1974-07-30 | Fungicidal composition and process |
| AU71887/74A AU7188774A (en) | 1973-08-11 | 1974-07-31 | Fungicide |
| NL7410376A NL7410376A (nl) | 1973-08-11 | 1974-08-01 | Werkwijze voor het bereiden van een fungicide. |
| IT52423/74A IT1050234B (it) | 1973-08-11 | 1974-08-02 | Fungicida |
| FR7427281A FR2239940B1 (enrdf_load_stackoverflow) | 1973-08-11 | 1974-08-06 | |
| ZA00745029A ZA745029B (en) | 1973-08-11 | 1974-08-07 | Fungicide |
| DK421574A DK421574A (enrdf_load_stackoverflow) | 1973-08-11 | 1974-08-08 | |
| SU2145698A SU538650A3 (ru) | 1973-08-11 | 1974-08-09 | Фунгицид |
| BE147455A BE818675A (fr) | 1973-08-11 | 1974-08-09 | Fongicide a base de nitro-3 isophtalate de diisopropyle |
| DD180424A DD112338A5 (enrdf_load_stackoverflow) | 1973-08-11 | 1974-08-09 | |
| AT652474A ATA652474A (de) | 1973-08-11 | 1974-08-09 | Fungizid |
| CH1091474A CH584002A5 (enrdf_load_stackoverflow) | 1973-08-11 | 1974-08-09 | |
| HUBA3124A HU169823B (enrdf_load_stackoverflow) | 1973-08-11 | 1974-08-09 | |
| PL1974173362A PL89911B1 (enrdf_load_stackoverflow) | 1973-08-11 | 1974-08-09 | |
| GB3515874A GB1469177A (en) | 1973-08-11 | 1974-08-09 | Fungicide |
| DK588275A DK588275A (da) | 1973-08-11 | 1975-12-23 | Fungicid |
| AT280876A ATA280876A (de) | 1973-08-11 | 1976-04-15 | Fugizid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732340741 DE2340741A1 (de) | 1973-08-11 | 1973-08-11 | Fungizid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2340741A1 true DE2340741A1 (de) | 1975-02-20 |
Family
ID=5889513
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19732340741 Pending DE2340741A1 (de) | 1973-08-11 | 1973-08-11 | Fungizid |
Country Status (17)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2830042A1 (de) * | 1977-10-01 | 1979-04-12 | Centrala Ind Prod Anorg | Fungizid |
| WO1982001980A1 (en) * | 1980-12-12 | 1982-06-24 | Pont Du | Agricultural and horticultural microbiocidal compositions |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2909550B1 (de) * | 1979-03-10 | 1980-05-08 | Bayer Ag | Mikrobizide Mittel und deren Verwendung |
| AU2002239395A1 (en) * | 2000-11-01 | 2002-06-03 | The Procter And Gamble Company | Hiv treatment with benzimidazoles |
| AU2003220585A1 (en) * | 2002-03-26 | 2003-10-13 | Arizona Board of Regents on behalf of the University of Arizone | Solubilization of weak bases |
| EP1563733A1 (en) * | 2004-02-12 | 2005-08-17 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting mitosis and cell division |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3745187A (en) * | 1967-10-30 | 1973-07-10 | Nippon Soda Co | Bis-thioureido-benzenes and preparation thereof |
-
1973
- 1973-08-11 DE DE19732340741 patent/DE2340741A1/de active Pending
-
1974
- 1974-07-19 JP JP49082321A patent/JPS5088228A/ja active Pending
- 1974-07-30 US US05/493,099 patent/US3954993A/en not_active Expired - Lifetime
- 1974-07-31 AU AU71887/74A patent/AU7188774A/en not_active Expired
- 1974-08-01 NL NL7410376A patent/NL7410376A/xx unknown
- 1974-08-02 IT IT52423/74A patent/IT1050234B/it active
- 1974-08-06 FR FR7427281A patent/FR2239940B1/fr not_active Expired
- 1974-08-07 ZA ZA00745029A patent/ZA745029B/xx unknown
- 1974-08-08 DK DK421574A patent/DK421574A/da unknown
- 1974-08-09 PL PL1974173362A patent/PL89911B1/xx unknown
- 1974-08-09 CH CH1091474A patent/CH584002A5/xx not_active IP Right Cessation
- 1974-08-09 AT AT652474A patent/ATA652474A/de not_active Application Discontinuation
- 1974-08-09 DD DD180424A patent/DD112338A5/xx unknown
- 1974-08-09 SU SU2145698A patent/SU538650A3/ru active
- 1974-08-09 GB GB3515874A patent/GB1469177A/en not_active Expired
- 1974-08-09 HU HUBA3124A patent/HU169823B/hu unknown
- 1974-08-09 BE BE147455A patent/BE818675A/xx unknown
-
1975
- 1975-12-23 DK DK588275A patent/DK588275A/da unknown
-
1976
- 1976-04-15 AT AT280876A patent/ATA280876A/de not_active IP Right Cessation
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2830042A1 (de) * | 1977-10-01 | 1979-04-12 | Centrala Ind Prod Anorg | Fungizid |
| WO1982001980A1 (en) * | 1980-12-12 | 1982-06-24 | Pont Du | Agricultural and horticultural microbiocidal compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| DD112338A5 (enrdf_load_stackoverflow) | 1975-04-12 |
| DK421574A (enrdf_load_stackoverflow) | 1975-04-14 |
| ZA745029B (en) | 1975-09-24 |
| US3954993A (en) | 1976-05-04 |
| BE818675A (fr) | 1975-02-10 |
| NL7410376A (nl) | 1975-02-13 |
| PL89911B1 (enrdf_load_stackoverflow) | 1976-12-31 |
| JPS5088228A (enrdf_load_stackoverflow) | 1975-07-15 |
| SU538650A3 (ru) | 1976-12-05 |
| GB1469177A (en) | 1977-03-30 |
| DK588275A (da) | 1975-12-23 |
| AU7188774A (en) | 1976-02-05 |
| FR2239940B1 (enrdf_load_stackoverflow) | 1977-10-14 |
| FR2239940A1 (enrdf_load_stackoverflow) | 1975-03-07 |
| HU169823B (enrdf_load_stackoverflow) | 1977-02-28 |
| ATA652474A (de) | 1976-07-15 |
| IT1050234B (it) | 1981-03-10 |
| CH584002A5 (enrdf_load_stackoverflow) | 1977-01-31 |
| ATA280876A (de) | 1976-08-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2656747A1 (de) | Morpholinderivate | |
| EP0003211B1 (de) | Verfahren zur Bekämpfung von Insekten mit Imidazolderivaten | |
| DE3308806A1 (de) | Fungizide mittel, substituierte glucopyranosylamine und verfahren zur bekaempfung von pilzen | |
| EP0000333B1 (de) | Derivate cyclischer Amine und diese enthaltende Fungizide | |
| EP0007479B1 (de) | N-Arylpropyl-substituierte cyclische Amine, Fungizide, die diese Verbindungen enthalten und Verfahren zu ihrer Herstellung | |
| EP0006992A1 (de) | 3-(p-Isopropyl-phenyl)-2-methyl-n-propyl-amine, diese enthaltende Fungizide, ein Verfahren zur Herstellung der genannten Verbindungen und Verfahren zur Bekämpfung von Pilzen unter Verwendung der genannten Verbindungen | |
| EP0002222A1 (de) | Aralkylpiperidinone und deren Anwendung als Fungizide | |
| DE2340741A1 (de) | Fungizid | |
| DE2755940C2 (de) | Mittel zur Regulierung des Pflanzenwachstums | |
| DE2329034C3 (de) | Fungizid auf Basis von Nitroisophthalsäureestergemischen | |
| DE2526308C2 (de) | 2-Halogen-5-trichlormethyl-1,3,4-thiadiazole | |
| EP0014999B1 (de) | Optisch aktive Formen des 4-(3-(p-tert.-Butylphenyl)-2-methyl-propyl)-cis-2,6-dimethyl-morpholins und ihre Salze; Fungizide, die diese Verbindungen enthalten, und Verfahren zu ihrer Herstellung | |
| DE3309765A1 (de) | Fungizide mittel | |
| DE2265312A1 (de) | Pyrimidinsulfamatderivate, deren herstellung und deren verwendung als fungizide | |
| DE2319362C3 (de) | Fungizides Mittel auf Basis von Dithiocarbamat und N-Tridecyl-2,6dimethylmorpholin | |
| DE2704962A1 (de) | Mittel zur beeinflussung des pflanzenwachstums | |
| DE3121349A1 (de) | Cyclohexenderivate, verfahren zu ihrer herstellung und diese enthaltende fungizide | |
| DE2521405A1 (de) | Fungizid | |
| EP0009091B1 (de) | Verfahren zur selektiven Bekämpfung von unerwünschtem Pflanzenwachstum mit herbiziden Mitteln auf Basis von Acetaniliden und N-Dichloracetyl-2,2-dimethyl-1,3-oxazolidin | |
| EP0077300B1 (de) | Triorganozinnhydantoin-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung | |
| EP0019769B1 (de) | Fungizid, enthaltend ein 3-Cyclohexan-1-amino-propanderivat, Verfahren zu seiner Herstellung und seine Verwendung zur Bekämpfung von Pilzen | |
| DE3001581A1 (de) | Substituierte n- (3(4'-tert-butyl-cyclohex-1'-en1'yl)-2-methyl-propyl-1) -cycloalkalamine, ihre herstellung und ihre anwendung als fungizide | |
| DE2334714A1 (de) | Schaedlingsbekaempfungsmittel | |
| DE2018248A1 (de) | Schädlingsbekämpfungsmittel | |
| DE1642218C (de) | Substituierte Thiocarbamate und deren Verwendung |